Variant #0000855629 (NC_000019.9:g.45900289G>C, NM_012099.1:c.-9666G>C (CD3EAP))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45900289G>C
DNA change (hg38) -
Published as PPP1R13L(NM_006663.4):c.226C>G (p.P76A)
ISCN -
DB-ID CD3EAP_000033
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPP1R13L NM_006663.3 -?/. - c.226C>G r.(?) p.(Pro76Ala)
CD3EAP NM_012099.1 -?/. - c.-9666G>C r.(?) p.(=)


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